Ni B, Stephenson D, Wu X, Smalstig E B, Clemens J, Paul S M
Division of Neuroscience Research, Lilly Research Laboratories, Eli Lilly and Co., Indianapolis, Indiana 46285, USA.
Brain Res Mol Brain Res. 1997 Aug;48(1):132-9. doi: 10.1016/s0169-328x(97)00090-9.
A recently identified neuronal Na+-dependent phosphate cotransporter (rBNPI) has been shown to import inorganic phosphate (P(i)) required for the production of high-energy phosphates which are vital to neuronal energy metabolism. In the present study, we have examined the expression of rBNPI mRNA in the hippocampus of rats subjected to 30 min of global ischemia by four-vessel occlusion. In situ hybridization reveals that transient forebrain ischemia results in a selective reduction in rBNPI mRNA expression in CA1 pyramidal neurons of the hippocampus. Expression of rBNPI is significantly reduced by 24 h and completely absent at 72 h following global ischemia when CA1 pyramidal neurons begin to show cell damage. By contrast, there is no change in the expression of Nedd2 mRNA, a developmentally regulated cell death gene, in CA1 pyramidal neurons at these same time points. The loss of rBNPI transcripts appears to be selective for CA1 pyramidal neurons since rBNPI mRNA expression is unchanged in neurons of the CA2-CA4 pyramidal cell layers following global ischemia. Our data indicate that an early reduction of rBNPI transcripts may contribute to a reduction in P(i)-dependent energy metabolism or signal transduction which has been reported in CA1 hippocampal neurons following global ischemia.
最近发现的一种神经元钠依赖性磷酸盐共转运体(rBNPI)已被证明可导入高能磷酸盐产生所需的无机磷酸盐(P(i)),而高能磷酸盐对神经元能量代谢至关重要。在本研究中,我们检测了通过四动脉闭塞法经历30分钟全脑缺血的大鼠海马中rBNPI mRNA的表达。原位杂交显示,短暂性前脑缺血导致海马CA1锥体神经元中rBNPI mRNA表达选择性降低。全脑缺血后24小时,rBNPI的表达显著降低,当CA1锥体神经元开始出现细胞损伤时,72小时时rBNPI完全缺失。相比之下,在这些相同时间点,CA1锥体神经元中Nedd2 mRNA(一种受发育调控的细胞死亡基因)的表达没有变化。rBNPI转录本的缺失似乎对CA1锥体神经元具有选择性,因为全脑缺血后CA2 - CA4锥体细胞层神经元中的rBNPI mRNA表达没有变化。我们的数据表明,rBNPI转录本的早期减少可能导致P(i)依赖性能量代谢或信号转导的降低,这在全脑缺血后的海马CA1神经元中已有报道。